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United States Patent |
5,242,962
|
Jahn
|
September 7, 1993
|
Fluoropolymer coating composition
Abstract
Aqueous fluoropolymer formulations containing in finely divided form from
15 to 75% by weight of a fluoropolymer which preferably has at least 40%
by weight of tetrafluoroethylene units, from 0.5 to 10% by weight of an
organic compound which has at least two, preferably 2-4, isocyanate groups
and, optionally, up to 20% by weight of auxiliary or additive substances
are prepared and used for coating yarn, in particular sewing yarn, and
textile sheet materials.
Inventors:
|
Jahn; Bernhard (Obermeitingen, DE)
|
Assignee:
|
Hoechst Aktiengesellschaft (Frankfurt am Main, DE)
|
Appl. No.:
|
307516 |
Filed:
|
February 2, 1989 |
Foreign Application Priority Data
Current U.S. Class: |
524/197; 524/545; 524/546 |
Intern'l Class: |
C08K 005/16 |
Field of Search: |
524/197,839,509,545,546,805
525/199
|
References Cited
U.S. Patent Documents
2968649 | Jan., 1961 | Pailthorp et al. | 526/254.
|
4347268 | Aug., 1982 | Close | 525/199.
|
4549921 | Oct., 1985 | Wolfe, Jr. | 525/121.
|
4692382 | Sep., 1987 | Schmitt et al. | 525/111.
|
4769413 | Sep., 1988 | Fleming et al. | 524/507.
|
Foreign Patent Documents |
62-022862 | Jan., 1987 | JP | 525/199.
|
Primary Examiner: Bleutge; John C.
Assistant Examiner: Sweet; Mark
Claims
I claim:
1. An aqueous fluoropolymer formulation containing in finely divided form
from 15 to 75% by weight of a fluoropolymer, from 0.5 to 10% by weight
based on the weight of the fluoropolymer formulation of an organic
compound having at least two isocyanate groups and up to 20% of an
auxiliary or additive substance.
2. The aqueous fluoropolymer formulation as claimed in claim 1, wherein the
fluoropolymer has at least 40% by weight of tetrafluoroethylene units.
3. The aqueous fluoropolymer formulation as claimed in claim 1, wherein the
fluoropolymer has from 40 to 60% by weight of tetrafluoroethylene units,
from 10 to 30% by weight of hexafluoropropylene units and from 20 to 40%
by weight of vinylidene fluoride units.
4. The aqueous fluoropolymer formulation as claimed in claim 1, wherein the
organic substance which has at least two isocyanate groups contains from 2
to 4 isocyanate groups.
5. The aqueous fluoropolymer formulation as claimed in claim 1, wherein the
organic compound which has at least two isocyanate groups is a derivative
of diisocyanatotoluene or is a tris(isocyanatoalkyl)biuret.
6. The aqueous fluoropolymer formulation as claimed in claim 1, wherein the
organic compound which has at least two isocyanate groups is the
dimerization trimerization product of 2,4-diisocyanatotoluene.
7. The aqueous fluoropolymer formulation as claimed in claim 1, wherein
there is present as an auxiliary or additive substance a wetting agent, a
dispersant and/or a stabilizer.
8. An aqueous fluoropolymer formulation as claimed in claim 1, which
consists essentially of:
an aqueous dispersion medium containing up to 20% by weight based on the
weight of the fluoropolymer formulation of an auxiliary or additive
substance, and
homogenously dispersed in said aqueous dispersion medium, from 15 to 75% by
weight of said fluoropolymer, the amount and degree of dispersion of said
fluoropolymer being sufficient to provide an aqueous paste, and from 0.5
to 10% of a finely divided organic compound having at least two isocyanate
groups.
Description
DESCRIPTION
The present invention relates to an aqueous fluoropolymer formulation and
to the preparation thereof, this fluoropolymer formulation making it
possible to produce strongly adherent fluoropolymer coatings on textile
materials made of organic synthetic fibers.
European Patent Application 0,224,262 disclosed laminating textile sheet
materials on both sides with a polyvinyl fluoride coating. In this known
process, a solution of the polymer in an organic solvent is cast on a
conveyor belt into a thin layer which is made to gel by heating. The gel
layer is then pressed onto the surface of the textile material to be
laminated. In this process, the fluoropolymer coating is fixed to the
textile material only at the surface and virtually no impregnation of the
individual filaments with the fluoropolymer takes place.
German Offenlegungsschrift 3,301,270 discloses a process for sheathing
fiber or filament yarns with a fluorine-containing polymer. In this
resource-intensive process, the filament to be sheathed is pulled through
a central hole in an annular spinneret while at the same time a tube of
fluoropolymer is extruded from the annular spinneret. The extruded tube
therefore surrounds the filament drawn out of the central hole as a
loose-fitting sheath. No firm bonding takes place between the
fluoropolymer tube and the filament sheathed therewith.
It is also known for the manufacture of awnings, air-houses, flexible
containers and similar products to coat textile sheet structures, usually
woven fabrics, preferably those made of synthetic organic fibers or
filaments, with polymer materials, usually with polyvinyl chloride (PVC).
This coating is effected by impregnating the textile materials in
suspensions of polyvinyl chloride in organic liquids. In the course of
this coating, even the individual filaments of the textile material become
enveloped by the polyvinyl chloride coating. To obtain sufficient adhesion
between the polyvinyl chloride coating and the synthetic fibers, the
coating is carried out in two stages. First a basecoat is applied
comprising a mixture of a PVC paste or suspension with an adhesion
promotor; this is followed by the application of a top-coat comprising a
pure PVC formulation. The adhesion promotors suitable for this purpose are
known. It is usual to use two-component adhesives comprising an organic
substance having a plurality of hydroxyl groups, preferably a
hydroxyl-containing polyester, and an organic substance having a plurality
of isocyanate groups.
It is also already known to coat materials such as threads or sheetlike
structures made of organic synthetic fibers with fluoropolymers in order
to confer particularly advantageous properties, for example a low
co-efficient of friction, a high chemical resistance and a soil-repellent
effect, on their surfaces. To this end, the synthetic fiber materials are
impregnated or coated with commercially available aqueous dispersions of
fluoropolymers and the resulting polymeric coating is fixed by means of a
heat treatment.
However, in order to make composite materials based on
fluoropolymer-treated synthetic fibers suitable for a wide range of
applications, for example the manufacture of membranes for textile
construction, flexible containers, conveyor belts, fabric tubes and the
like, it is absolutely necessary that the fluoropolymer should show
adequate adhesive strength to the synthetic fiber. Adhesive strength is
here to be understood as meaning the resistance to separation of base
material and coating for a 5 cm wide strip as determined in line with
German Standard Specification DIN 53 530. Adequate performance capability
of the composite is ensured when, depending on the intended use, adhesion
values of from 10 to 15 daN/5 cm are obtained.
However, the production of strongly adherent fluoropolymer coatings of
synthetic fiber materials presents even greater difficulties than the
production of polyvinyl chloride coatings. This is because it is found
that fluoropolymers are far more inert with respect to synthetic fibers,
for example polyester fibers, polyamide fibers or aramid fibers, than
polyvinyl chloride; that is, they show great reluctance to enter permanent
physical or chemical bonds with synthetic fiber surfaces. Moreover,
fluoropolymers which, on the basis of the physical data, might be thought
suitable for use as coating agents for synthetic fibers are in general
commercially available in the form of aqueous dispersions or pastes. It is
therefore not possible using these known fluoropolymer dispersions or
pastes to produce coatings on synthetic fiber materials showing adequate
adhesive strength for all the abovementioned industrial uses.
Nor is it possible to obtain a significant improvement in the adhesion of
fluoropolymer coatings by using the one-or two-component adhesion
promotors used successively in the production of PVC coatings.
It has now been found, surprisingly, that it is possible to produce very
strongly adherent fluoropolymer coatings on synthetic fibers by applying
at least as the first impregnation or as the first coat (basecoat) a
fluoropolymer formulation which, in place of conventional adhesion
promotors, merely contains an organic compound having a plurality of
isocyanate groups.
The present invention thus provides an aqueous fluoropolymer formulation
containing in finely divided form from 15 to 75% by weight, preferably
from 25 to 60% by weight, of a fluoropolymer, from 0.5 to 10, preferably
from 1 to 5, % by weight of an organic compound which has at least two,
preferably 2 to 4, isocyanate groups and, optionally, up to 20% by weight,
preferably up to 10% by weight, of auxiliary or additive substances.
The fluoropolymers of the formulation according to the invention contain to
an extent of at least 40% tetrafluoroethylene units and to an extent of up
to 60% units derived from other unsaturated fluorine-containing monomers
copolymerizable with tetrafluoroethylene. Advantageously, the amounts and
identities of the fluorine-containing monomers copolymerized with the
tetrafluoroethylene are chosen in such a way that the copolymer has the
desired mechanical properties, such as strength, flexibility, elasticity,
low slip friction and the like, and also good chemical resistance. More
particularly, the composition should be chosen in such a way that the
fluoropolymer is readily dispersible in water and also gives dispersions
of good long term stability. Preference here is given to those
fluoropolymers whose melting points are below the melting point of the
synthetic fibers to be finished with the formulation. More particularly,
fluoropolymers of advantage there are those whose melting points are from
5.degree. to 50.degree., preferably from 20.degree. to 40.degree. C.,
below the melting point of the synthetic fibers to be finished.
High suitability within the meaning of the above specifications is
possessed by tetrafluoroethylene copolymers containing to an extent of up
to 60% units derived from hexafluoropropylene and vinylidene fluoride. A
fluoropolymer particularly suitable for preparing the fluoropolymer
formulation according to the invention contains from 40 to 60% by weight
of tetrafluoroethylene units, from 10 to 30% by weight of
hexafluoropropylene units and from 20 to 40% by weight of vinylidene
fluoride units.
The preparation of such fluoropolymers is known, and numerous
representatives of this class of compounds are commercially available.
Particularly high suitability for the preparation of the fluoropolymer
formulation according to the invention and for producing strongly adherent
fluoropolymer coatings on synthetic fibers is possessed by the range of
.RTM.Hostaflon TFB products available from Hoechst AG.
Organic compounds which have a plurality of isocyanate groups and which can
be incorporated as adhesion promotors into the fluoropolymer formulations
according to the invention are known in large numbers, and numerous
representatives of this class of compounds are commercially available. A
number of industrially important tri- and polyisocyanates which are also
suitable for the use according to the invention may be found for example
in Ullmann's Enzyklopadie der technischen Chemie, 4th edition, Volume 13,
page 355, Volume 15, page 634 and Volume 19, pages 303 and 304. It is of
course also possible to use other di- and polyisocyanates which are
dispersible and sufficiently stable in aqueous systems in the
fluoropolymer formulations according to the invention. Preferred di- and
polyisocyanates are for example the isomeric 2,4-diisocyanatotoluenes and
mixtures thereof, 1,5-diisocyanatonaphthalene, diisocyanatodiphenylmethane
and its technical-grade isomer mixtures, dimerized and trimerized
diisocyanatotoluene, and adducts of diisocyanatotoluene with
trimethylolpropane and tris[isocyanatohexyl]biuret. Particular preference
for use in the fluoropolymer formulations according to the invention is
given to the aforementioned derivatives of diisocyanatotoluene, in
particular its dimerization product, which is available from Bayer AG
under the name .RTM.Desmodur TT.
As additives there may be present in the fluoropolymer formulations
according to the invention various auxiliary and additive substances.
These include in particular surface-active agents (surfactants) which may
serve as wetting agents in the preparation of formulations and in their
application and dispersants which facilitate and/or make possible the
dispersion of fluoropolymers and cyanato-containing compounds in the
aqueous phase and increase dispersion stability. Again such surface-active
agents are described in the literature in large numbers.
We cite for example Ullmann's Enzyklopadie der technischen Chemie, 4th
edition, Volume 22, pages 455 et seq., in particular pages 466 and 488 and
also Volume 23, page 120. It is possible to use for example anionic,
cationic or amphoteric surfactants, but preferably nonionic surfactants
derived from ethoxylates, terminally blocked ethoxylates, fatty acid
esters and polyhydroxy compounds. The possibilities also include
silicone-based surfactants or fluorosurfactants. If a novel fluoropolymer
formulation having a relatively low fluoropolymer concentration and a
correspondingly low viscosity is to be used, it can be advantageous also
to add as an auxiliary and additive substance a thickening or
antimigration agent, for example agents from the group of the
carboxymethylated polysaccharides, xanthans or alginates, of the starch or
cellulose derivatives, of the acrylate copolymers or of polyvinyl alcohol.
Even inorganic thickening agents such as pyrogenic silica or bentonites
may be incorporated into the fluoropolymer formulation according to the
invention in low concentration.
For specific applications, in particular for the topcoat, it is also
possible to use mixtures of formulations according to the invention with
blend components specific to the intended use. Such blend components are
for example pigments, fillers, flame-retardant agents and modifying agents
which are capable of modifying the properties of the fluoropolymer
coating, for example plasticizers, lubricants or agents which modify the
surface properties. These can be incorporated into the formulations
according to the invention in a total amount of up to 25% by weight,
preferably up to 15% by weight. However, it is advantageous not to use
this second group of additives in formulations according to the invention
which are to be used in the first coat (the basecoat).
It is of course advantageous and particularly preferable to choose the
amount of the auxiliary or additive substances in the fluoropolymer
formulations according to the invention in such a way that the effect
intended with these additives is obtained to an optimum degree.
The fluoropolymer formulation according to the invention is prepared in a
conventional manner by homogenizing, if 100 parts by weight of the
formulation are to be prepared, from 15 to 75 parts by weight of
fluoropolymer, from 0.5 to 10 parts by weight of the organic compound
having at least two isocyanate groups and, optionally, up to 20 parts by
weight of further auxiliary or additive substances in finely divided form
with sufficient water to make up to 100 parts by weight, in a suitable
mixing apparatus. If the fluoropolymers used here are solid, they must
first be converted into a very finely divided form and then by vigorous
stirring or kneading into a uniform dispersion or paste in the requisite
amount of water, if necessary with the addition of a sufficient amount of
dispersing auxiliaries and/or wetting agents. At the same time or
thereafter the requisite amount of the selected organic compound
containing a plurality of cyanate groups is added.
The mixing operation is advantageously carried out at room temperature or
at an only moderately elevated temperature. Further additive or auxiliary
substances may be added to the blend batches from the start, or they may
be incorporated once a stable fluoropolymer dispersion or paste has been
obtained.
It is advantageous to prepare the fluoropolymer formulations according to
the invention by incorporating into an aqueous fluoropolymer suspension or
fluoropolymer paste which may contain further auxiliary or additive
substances from 0.5 to 10% by weight, based on the final weight of the
mixture, a finely divided form of the organic substance which contains at
least two isocyanate groups, and homogenizing it. Aqueous fluoropolymer
suspensions or pastes which are highly suitable for producing the
formulations according to the invention are for example the commercially
available .RTM.Hostaflon TFB range mentioned above.
Textile materials for the purposes of this invention can be one- or
two-dimensional; that is, they are threads or else settlelike structures,
for example woven fabrics, knitted fabrics, laid fabrics or nonwoven
fabrics of various thicknesses, or even laminates of identical or
different sheetlike structures of this type, possibly combined with other
raw materials.
The filaments or fibers of the textile materials to be coated can by dyed
or undyed, smooth or textured. There is no evidence that commercial
textile dyes migrate out of the synthetic fibers into the fluoropolymer
coating.
In principle, the fluoropolymer formulation according to the invention can
be applied in one operation to the synthetic fiber material to be coated.
To produce thicker fluoropolymer coats, the fluoropolymer formulation
according to the invention is advantageously applied in a plurality of
operations, in which case, depending on the chosen composition of the
formulation and the associated consistency, an impregnation by dipping or
padding or alternatively a paste application, for example by knife-coating
or roller-coating, may be carried out. In this advantageous application of
the formulation according to the invention it is particularly advantageous
to carry out the first application, i.e. the production of the basecoat,
with a fluoropolymer formulation according to the invention which, aside
from the organic compound having a plurality of isocyanate groups,
contains no or only little other additives, in particular no solid
additives, for example pigments or flame-retardant additives.
It is also possible to prepare fluoropolymer coatings on organic synthetic
fibers by using the fluoropolymer formulation according to the invention
only to prepare the basecoat and to use for the basecoat or basecoats a
normal aqueous fluoropolymer dispersion or paste which is free of
isocyanato-containing organic compounds but which, of course, may contain
further additives, for example dispersants, wetting agents, pigments,
flame-proofing agents or other filling and auxiliary substances.
As stated above, it is also possible to carry out the fluoropolymer finish
using the fluoropolymer formulation according to the invention in a single
step, for example by impregnating, this being advantageous in particular
in the application to threads made of synthetic filaments or fibers. In
the application of the fluoropolymer formulation according to the
invention, each application by impregnation or coating is in general
followed by a heat treatment of the material to dry the application and to
fix the freshly applied fluoropolymer to the substrate.
The fluoropolymer coatings applied to the above-specified application
methods have a high adhesive strength of at least 10 daN/5 cm, on use of
preferred formulations according to the invention in general more than 20
daN/5 cm. The adhesive strength of the fluoropolymer to the synthetic
fiber can be controlled by the amount which is added of the organic
compound containing two or more isocyanate groups. Furthermore, the
adhesive strength can be influenced by the temperature and duration of the
heat treatment carried out following application of the formulation
according to the invention.
The present invention also provides the textile sheet materials, for
example woven fabrics, knitted fabrics, laid fabrics or nonwoven fabrics
made of synthetic fibers, preferably polyesters, polyamide or aramid
fibers, in particular polyester fibers, which are coated with the
fluoropolymeric formulation according to the invention. Textile sheet
materials for the purposes of the present invention also include laminates
of identical or different sheetlike structures, including any mixtures
with other raw materials. The coated sheetlike structures are notable for
having, at least in the fluoropolymer layer directly adjoining the fiber
surface, one or more adhesion-promoting constituents derived from an
organic compound having at least two isocyanate groups. Furthermore, the
fluoropolymer-coated synthetic fiber textile materials according to the
invention are notable for the fact that the coating has an adhesive
strength, as measured in line with German Standard Specification DIN 53
530, of at least 10 daN/5 cm. Owing to the high mechanical strength
properties of polyester, polyamide or aramid fibers, the materials which
have been fluoropolymer-coated according to the invention also have
excellent mechanical strength values which very much widen their range of
possible industrial uses. Moreover, the coated materials have low
coefficients of friction, show high chemical resistance and are
soil-repellent.
The present invention further provides the synthetic fiber threads coated
with the fluoropolymer formulation according to the invention. The term
threads is here to be understood as meaning monofilaments, multifilament
yarns or even staple fiber yarns. Suitable fiber material here too
comprises in particular polyester, polyamide or aramid synthetic fibers,
preferably polyester fibers. The fluoropolymer-coated yarns thus obtained
have not only the high mechanical strength values characteristic of
synthetic fibers but also a particularly high-slip, chemically resistant
and soil-repellent surface.
The fluoropolymer formulations according to the invention prove
particularly useful for the bonding of sewing yarn. This is to be
understood as meaning that the fluoropolymer coating brings about a
flexible bond between the individual filaments of the yarn. The bonded
sewing yarns thus produced have a particularly high strength and excellent
sewing properties. A particular advantage here is that the bonding action
of the extremely inert fluoropolymer coating does not disappear on dyeing
or on application of sewing finishes.
The threads coated according to the invention and the bonded sewing yarn
are also notable for the fact that they have, at least in the
fluoropolymer layer immediately adjoining to the fiber surface, one or
more adhesion-promoting constituents which are derived from an organic
compound having at least two isocyanate groups and that the fluoropolymer
coating has such adhesive strength that it does not become detached due to
mechanical stress such as is experienced in the further processing of the
threads or in the course of the intended use of the sewing yarn, for
example in the course of winding, weaving or knitting or in the course of
sewing.
The working examples that follow illustrate the preparation of the
fluoropolymer formulation according to the invention and its application
to yarn and textile sheet materials.
EXAMPLE 1
500 g of a commercially available 50% strength by weight aqueous paste of a
fluorocopolymer of tetrafluoroethylene, hexafluoropropylene and vinyl
difluoride (.RTM.Hostaflon TFB X 7900 from Hoechst AG) containing 2% by
weight of a thickener based on an acrylate polymer and 15 g of a finely
pulverulent
1,3-bis-(4-methyl-3-isocyanatophenyl)-1,3-diazacyclobutane-2,4-dione (for
example Desmodur TT from Bayer AG) are kneaded for 15 minutes in a kneader
at 20.degree.-25.degree. C. and packaged. This gives a pasty fluoropolymer
formulation which is highly suitable for coating textile materials (yarn
or textile sheet material) made of synthetic fibers. It contains 48.5% by
weight of fluoropolymer, 2.9% by weight of the diisocyanato compound and
1.9% by weight of thickener. The formulation can also be used to good
effect as a primer coating in the coating of textile materials onto which
firmly adherent fluoropolymer topcoats can be applied by means of
commercially available fluoropolymer pastes or dispersions.
EXAMPLE 2
10 g of wetting and dispersing agent based on an ethoxylated alkylphenol
are dissolved with vigorous stirring in 315 ml of demineralized water at
40.degree. C. 175 g of a finely ground fluorocopolymer of 55% by weight of
tetrafluoroethylene, 15% by weight of hexafluoropropylene and 30% by
weight of vinylidene fluoride are then slowly introduced with stirring.
Stirring is continued until the dispersion is completely homogenized, and
the dispersion is then packaged. The 35% strength by weight aqueous
fluoropolymer formulation obtained is highly suitable for the dip
impregnation and the coating of textile sheet materials and in particular
yarns made of synthetic fibers.
EXAMPLE 3
Coating of Woven Polyester Fabric
A 220 gm/m.sup.2 woven polyester fabric with 9 ends and 9 picks of 1100
dtex per cm is initially provided with the following basecoat:
A fluoropolymer paste according to Example 1 is applied to both sides of
the fabric, in each case at a rate of 60-80 g/m.sup.2, by spread coating
by means of an air knife or a rubber blanket doctor blade.
The material is then sintered at 210.degree. C. for 2 minutes. Topcoating
is effected with a 50% strength .RTM.Hostaflon TFB X 7900 paste (aqueous
fluoropolymer pate) which, if desired, may additionally be pigmented or
flameproofed (for example by the addition of 5% of TiO.sub.2 and/or 10% of
Sb.sub.2 O.sub.3, based on solid fluoropolymer). This formulation is
applied by spread coating with a steel roll doctor or rubber blanket
doctor blade in a plurality of coats (for example 6 coats on the front, 4
coats on the back), each coat being followed by an intermediate drying at
210.degree. C. for 2 minutes.
The total amount applied to the front of the fabric is 300 g/m.sup.2 and to
the back of the fabric 160 g/m.sup.2.
After the last coat has been applied, the fabric is sintered at 210.degree.
C. in the course of a residence time of 10 minutes. Thereafter the surface
of the front is embossed by means of a calender. The adhesive strength
obtained is 20.7 daN/5 cm.
If this example is repeated exactly as described above with a fluoropolymer
paste which contains no dicyanato compound but which otherwise has the
composition of the paste prepared in Example 1, an adhesive strength of
9.1 daN/5 cm is found on the front of the coated fabric and an adhesive
strength of 6.9 daN/5 cm on the back.
EXAMPLE 4
Fabric: as in Example 3.
Basecoat: as in Example No. 3, the basecoat being sintered at 210.degree.
C. in the course of a residence time of 10 minutes.
Topcoating: as in Example 3.
Adhesive strength obtained: 30.2 daN/5 cm.
EXAMPLE 5
Fabric: as in Example 3.
Basecoat: as in Example No. 4.
Topcoating:
Formulation: Hostaflon TFB X 7100 Melt granules+5% of TiO.sub.b +10 % of
Sb.sub.2 O.sub.3 +1% of Hoechst Wax OP.
Application method: roll melt unit.
Amount replied:
front 300 g/m.sup.2
back 160 g/m.sup.2.
Processing conditions:
Roll temperatures: 205.degree. C.,
Preheat roll: 150.degree. C., IR radiator: 90%,
Machine speed: 3 m/minute,
Rubber roll pressure: 7 bar,
Film weight:
front 300 g/m.sup.2,
back 160 g/m.sup.2.
Adhesive strength obtained: 21.5 daN/5 cm.
EXAMPLE 6
Bonding of a Sewing Thread
A black 266-dtex 64-filament 3-ply polyethylene terephthalate yarn is
impregnated with 15-20% by weight (dry add-on based on weight of fiber) of
a formulation as described in Example 2 by dipping.
The impregnated thread is then heat-treated in a hot oven at 220.degree. C.
for at least 60 seconds. The sewing thread obtained does not show a change
in hue, nor any migration of the dye into the bonding. It produces very
good sewing results even under high stress, for example in industrial
sewing machines. No abrasion takes place either in winding or in sewing,
nor, following prolonged storage in bobbin form, is there any adhesive
coalescing of yarn layers.
In the same way, the above-described dip impregnation can also be effected
with a commercially available 35% strength fluoropolymer dispersion
(.RTM.Hostaflon TFB X 7100 from Hoechst AG) into which 1.5% by weight of
1,3-bis-(4-methyl-3-isocyanatophenyl)-1,3-diazacyclobutane-2,4-dione (for
example .RTM.Desmodur TT from Bayer AG) has been homogeneously
incorporated beforehand.
To test the quality of the sewing thread produced, it is subjected to a
tough sewing test such as that described in DE Offenlegungsschrift
3,431,834.
In this test, the thread is used in sewing under the following conditions:
industrial sewing machine Pfaff 363, stitch length 1 mm, zigzag seam 8 mm
width, 3,250 cycles/minute, 200 cN pre-tension, 4 layers of cotton twill.
The thread bonded according to the invention permits in this test on
average over 4,000 stitches without thread breakage, while an unbonded
thread permits on average only about 300 stitches.
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